Iron supplementation inhibits cough associated with ACE inhibitors

被引:23
作者
Lee, SC [1 ]
Park, SW [1 ]
Kim, DK [1 ]
Lee, SH [1 ]
Hong, KP [1 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Cardiol, Seoul 135710, South Korea
关键词
angiotensin-converting enzyme inhibitors; cough; iron;
D O I
10.1161/01.HYP.38.2.166
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Dry cough is the most common limiting factor of ACE inhibitor (ACEI) use. Generation of NO, a proinflammatory substance on bronchial epithelial cells, is increased by ACEI Using a randomized, double-blind, placebo-controlled trial, we tested the hypothesis that supplementing iron, an inhibitor of NO synthase, may reduce the cough associated with ACEI use. The subjects were 19 patients who had developed ACEI-induced cough. After a 2-week observation period, they were randomized to a daily morning dose of either 256-mg ferrous sulfate as a tablet or placebo for a treatment period of 4 weeks. The subjects were requested to rill out a cough diary by scoring the daily severity of the cough on a scale of 0 to 4. Mean daily cough scores for the last week of the observation and treatment period were compared. Changes in blood cell count and serum iron and ferritin concentration between the 2 periods were evaluated. Mean daily cough scores during the observation and treatment periods were 3.07 +/-0.70 and 1.69 +/-1.10, respectively, for the iron group and 2.57 +/-0.80 and 2.35 +/-1.22, respectively, for the placebo group, showing a significant reduction in cough scores with iron supplementation (P<0.01) but not with placebo. Three subjects in the iron group showed almost complete cough abolition. No significant changes in laboratory data were observed in either group. In conclusion, iron supplementation successfully decreases ACEI-induced cough. This effect may be related to the decrease of NO generation associated with the inhibition of NO synthase activity in bronchial epithelial cells.
引用
收藏
页码:166 / 170
页数:5
相关论文
共 34 条
[1]   CONSTITUTIVE AND INDUCIBLE NITRIC-OXIDE SYNTHASE GENE-EXPRESSION, REGULATION, AND ACTIVITY IN HUMAN LUNG EPITHELIAL-CELLS [J].
ASANO, K ;
CHEE, CBE ;
GASTON, B ;
LILLY, CM ;
GERARD, C ;
DRAZEN, JM ;
STAMLER, JS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (21) :10089-10093
[2]  
CANNON RO, 1998, AM J CARDIOL, V82, P8
[3]  
CASCIERI MA, 1984, MOL PHARMACOL, V25, P287
[4]  
CLANCY RM, 1995, P SOC EXP BIOL MED, V210, P93
[5]   Nitric oxide production in human inflammatory processes [J].
Dugas, B ;
Kolb, JP .
RESEARCH IN IMMUNOLOGY, 1995, 146 (09) :661-663
[6]  
FLAK TA, 1996, AM J RESP CRIT CARE, V154, P202
[7]  
FOGARI R, 1992, J CARDIOVASC PHARM, V19, P670
[8]   Bradykinin-evoked sensitization of airway sensory nerves: A mechanism for ACE-inhibitor cough [J].
Fox, AJ ;
Lalloo, UG ;
Belvisi, MG ;
Bernareggi, M ;
Chung, KF ;
Barnes, PJ .
NATURE MEDICINE, 1996, 2 (07) :814-817
[9]   Molecular biology of nitric oxide synthases [J].
Geller, DA ;
Billiar, TR .
CANCER AND METASTASIS REVIEWS, 1998, 17 (01) :7-23
[10]  
GILCHRIST NL, 1989, J HUM HYPERTENS, V3, P451